Research
Tag

Drug Metabolism

120 genetic variants with this tag.

RSID Gene Description Category
rs1042713 ADRB2 Arg16Gly Beta-2 adrenergic receptor variant affecting receptor downregulation, exercis... Fitness & Body Strong
rs10509679 CYP2C9 Intronic CYP2C9 haplotype tag associated with increased ischemic stroke risk ... Coronary Artery Disease & Atherosclerosis Emerging
rs10305492 GLP1R A316T Rare protective missense variant in the GLP-1 receptor associated with lower ... Pharmacogenomics Strong
rs10403955 CYP2B6 Intronic CYP2B6 haplotype-tagging variant associated with altered plasma conc... Pharmacogenomics Moderate
rs11854484 SLC28A2 SLC28A2 Pro22Leu Missense variant in the concentrative nucleoside transporter 2 (CNT2) gene th... Vitamins & Nutrient Absorption Moderate
rs1045642 ABCB1 C3435T Synonymous variant in P-glycoprotein affecting drug efflux pump expression an... Pharmacogenomics Moderate
rs1057910 CYP2C9 *3 No-function CYP2C9 variant with major warfarin implications Pharmacogenomics Established
rs1058164 CYP2D6 Synonymous CYP2D6 variant that promotes exon 3 skipping, reducing functional ... Pharmacogenomics Moderate
rs1058932 CYP2C8 CYP2C8 3-prime UTR variant associated with cardiovascular risk via altered ep... Pharmacogenomics Moderate
rs2032582 ABCB1 G2677T/A (Ser893Ala/Thr) Triallelic missense variant in the P-glycoprotein efflux pump that reduces th... Gamete Quality & DNA Repair Moderate
rs1065852 CYP2D6 *10 Decreased function CYP2D6 variant common in Asian populations Pharmacogenomics Established
rs1080985 CYP2D6 *2A promoter CYP2D6 promoter variant (-1584C>G) that reduces enzyme expression; the C alle... Pharmacogenomics Strong
rs1800629 TNF -308 G>A Promoter variant increasing TNF-alpha production approximately 2-fold, associ... TNF, NF-kB & Inflammatory Cytokines Strong
rs1051296 SLC19A1 SLC19A1 variant (RFC1) 3'UTR variant in the reduced folate carrier that affects miR-595 binding, alt... Methylation & Detox Moderate
rs1113129 CYP2C8 Intronic tagging SNP for CYP2C8 haplotype C, a low-activity haplotype associa... Pharmacogenomics Moderate
rs1051298 SLC19A1 SLC19A1 3'UTR variant (c.*746C>T) 3'UTR variant in the folate transporter gene affecting pemetrexed toxicity ri... Methylation & Detox Moderate
rs1142345 TPMT *3C No-function variant causing deficient thiopurine methylation; most common TPM... Pharmacogenomics Established
rs116855232 NUDT15 Arg139Cys Nucleotide diphosphatase that inactivates toxic thiopurine metabolites; reduc... Pharmacogenomics Established
rs2968864 KCNH2 KCNH2 QT interval GWAS variant (7q36.1) Intergenic variant at 7q36.1 near KCNH2 (hERG potassium channel) that modulat... Arrhythmia & Heart Rhythm Strong
rs12248560 CYP2C19 *17 Increased function CYP2C19 variant - rapid/ultrarapid metabolizer Pharmacogenomics Established
rs12721627 CYP3A4 *16 Missense variant reducing CYP3A4 enzyme activity by 50–74% depending on subst... Pharmacogenomics Moderate
rs12721629 CYP3A4 *16B Missense variant causing substrate-dependent reduced CYP3A4 activity, most pr... Pharmacogenomics Moderate
rs12044852 CD58 Intronic CD58 variant in strong LD with rs2300747 (r²=0.929); the C allele dr... Neurology & Cognition Strong
rs12980275 IFNL3 Downstream variant near IFNL3 — third IL28B locus predictor of hepatitis C sp... Pharmacogenomics Established
rs1341162 CYP2C8 Intronic CYP2C8 haplotype-tagging variant linked to altered drug metabolism c... Pharmacogenomics Moderate
rs1341164 CYP2C8 Intronic CYP2C8 variant tagging a haplotype associated with altered taxane dr... Pharmacogenomics Emerging
rs2231137 ABCG2 ABCG2 V12M (Val12Met) Missense variant in the ABCG2 transporter that impairs membrane localization ... Coronary Artery Disease & Atherosclerosis Moderate
rs2413775 SLC28A2 Promoter variant that increases SLC28A2/CNT2 transcription via enhanced HNF1 ... Vitamins & Nutrient Absorption Emerging
rs16947 CYP2D6 *2 Common CYP2D6 variant defining the *2 allele; previously considered normal-fu... Pharmacogenomics Strong
rs1208 NAT2 R268K NAT2 acetylation speed tag SNP - marks rapid vs slow acetylator haplotypes Methylation & Detox Established
rs17002852 CYP2D6 Synonymous CYP2D6 variant that causes allele dropout in standard CYP2D6*3 gen... Pharmacogenomics Moderate
rs12659 SLC19A1 Synonymous variant in the folate transporter SLC19A1 — a haplotype tag linked... Methylation & Detox Emerging
rs1799853 CYP2C9 *2 Decreased function variant affecting warfarin, phenytoin, and NSAIDs Pharmacogenomics Established
rs33980500 TRAF3IP2 D10N Missense variant in Act1 that abolishes IL-17 signaling by disrupting TRAF6 b... Psoriasis & Spondyloarthropathy Strong
rs1799971 OPRM1 A118G Mu-opioid receptor variant affecting opioid response, pain sensitivity, and p... Pharmacogenomics Strong
rs6742078 UGT1A10 Intronic variant in the UGT1A gene cluster (chromosome 2q37) strongly associa... Uric Acid & Kidney Function Strong
rs1800460 TPMT *3B Decreased-function variant causing reduced thiopurine methylation; pairs with... Pharmacogenomics Established
rs5186 AGTR1 A1166C 3' UTR variant in angiotensin II type 1 receptor affecting blood pressure reg... Blood Pressure & Hypertension Moderate
rs1800462 TPMT *2 The original TPMT deficiency allele — a no-function star allele causing ~100-... Pharmacogenomics Established
rs1801272 CYP2A6 *2 (L160H) Loss-of-function CYP2A6 variant that abolishes nicotine metabolism, slowing c... Pharmacogenomics Established
rs1934951 CYP2C8 Intronic CYP2C8 variant associated with paclitaxel-induced toxicity and bisph... Pharmacogenomics Moderate
rs72551348 UGT1A1 Q331R Rare pathogenic missense variant in the UGT1A1 gene that severely reduces bil... Uric Acid & Kidney Function Strong
rs1934953 CYP2C8 Intronic CYP2C8 variant linked to epoxygenase pathway activity, hypertension ... Pharmacogenomics Emerging
rs1934963 CYP2C9 Deep intronic CYP2C9 variant associated with altered drug response to sulfony... Pharmacogenomics Emerging
rs7594951 SRD5A2 SRD5A2 intron 4 regulatory variant Deep intronic variant in the testosterone-to-DHT converting enzyme; the minor... Reproductive Hormones Emerging
rs1934967 CYP2C9 Intronic CYP2C9 haplotype tag associated with altered warfarin sensitivity an... Pharmacogenomics Moderate
rs2066853 AHR Arg554Lys Aryl hydrocarbon receptor variant in the transactivation domain that alters A... Hormones & Sleep Moderate
rs1799930 NAT2 R197Q Slow acetylator variant affecting Phase II detoxification capacity Methylation & Detox Established
rs1934980 CYP2C8 Intronic CYP2C8 variant linked to altered enzyme expression and associated wi... Pharmacogenomics Moderate
rs2031920 CYP2E1 *5B (RsaI) Promoter variant increasing CYP2E1 inducibility, elevating oxidative stress f... Pharmacogenomics Moderate
rs2069526 CYP1A2 -739T>G Intronic CYP1A2 variant near the 5' end; G allele is associated with altered ... Pharmacogenomics Emerging
rs2070672 CYP2E1 CYP2E1 promoter variant affecting enzyme expression and susceptibility to ace... Pharmacogenomics Moderate
rs2070676 CYP2E1 Intronic CYP2E1 variant tagging the *1B haplotype; C allele marks reduced CYP... Pharmacogenomics Moderate
rs2108622 CYP4F2 V433M (*3) Reduces vitamin K metabolism, requiring higher warfarin doses to achieve anti... Pharmacogenomics Established
rs1800693 TNFRSF1A Splice-region variant in TNFR1 that generates a soluble Δ6 isoform mimicking ... Neurology & Cognition Strong
rs2231142 ABCG2 Q141K Reduces ABCG2 transporter function affecting rosuvastatin levels and uric aci... Pharmacogenomics Established
rs6311 HTR2A -1438G>A Regulatory variant in serotonin 2A receptor gene affecting SSRI side effects ... Mood & Behavior Moderate
rs1801280 NAT2 I114T Phase II detoxification - acetylation of aromatic amines and certain medications Methylation & Detox Established
rs2242480 CYP3A4 *1G Intronic variant in CYP3A4 intron 10 that upregulates a suppressive lncRNA, r... Pharmacogenomics Strong
rs2246709 CYP3A4 Intronic CYP3A4 variant associated with altered drug clearance, affecting met... Pharmacogenomics Moderate
rs2289669 SLC47A1 MATE1 G-1853A Intronic variant in MATE1, the renal and hepatic metformin efflux transporter... Pharmacogenomics Moderate
rs2480256 CYP2E1 3' UTR variant that increases CYP2E1 expression, raising hepatotoxicity risk ... Pharmacogenomics Moderate
rs2515641 CYP2E1 Synonymous exon-8 variant that reduces CYP2E1 mRNA and protein expression, al... Pharmacogenomics Moderate
rs887829 UGT1A1 UGT1A1*80 Promoter variant in UGT1A1 that tags the *28 reduced-expression haplotype; T ... Vascular Inflammation & Remodeling Strong
rs2740574 CYP3A4 *1B -392A>G Promoter variant affecting CYP3A4 expression, most common in African populations Pharmacogenomics Moderate
rs28371706 CYP2D6 *17 Decreased-function CYP2D6 allele common in African populations, reducing meta... Pharmacogenomics Established
rs28371725 CYP2D6 *41 Intronic splice variant causing decreased CYP2D6 enzyme activity through aber... Pharmacogenomics Established
rs28371733 CYP2D6 Rare CYP2D6 stop-gain variant (Glu418Ter) that eliminates enzyme activity, ca... Pharmacogenomics Established
rs28371759 CYP3A4 *18 (L293R) Rare missense variant causing a Leu293Arg substitution in CYP3A4, associated ... Pharmacogenomics Moderate
rs28399433 CYP2A6 *9 (TATA box) Promoter variant that reduces CYP2A6 expression by ~50%, slowing nicotine met... Pharmacogenomics Strong
rs28399444 CYP2A6 *7 (I471T) CYP2A6*7 missense variant that nearly abolishes nicotine C-oxidase activity; ... Pharmacogenomics Established
rs28695233 CYP2D6 Deep intronic CYP2D6 variant in intron 2 that serves as a haplotype tag in sp... Pharmacogenomics Emerging
rs316019 SLC22A2 Ala270Ser Reduces OCT2 organic cation transporter function in the kidney, lowering metf... Pharmacogenomics Moderate
rs2838956 SLC19A1 RFC1 intronic variant Intronic SLC19A1 variant that tags a haplotype affecting reduced folate carri... Methylation & Detox Emerging
rs35599367 CYP3A4 *22 Intronic splice variant causing ~50% reduced CYP3A4 mRNA expression, affectin... Pharmacogenomics Established
rs4410790 AHR Regulatory variant 54 kb upstream of the aryl hydrocarbon receptor gene; the ... Hormones & Sleep Strong
rs373489637 CYP2B6 V183G Near-complete loss-of-function CYP2B6 variant causing severely impaired metab... Pharmacogenomics Moderate
rs3745274 CYP2B6 516G>T Decreased-function variant affecting metabolism of efavirenz, methadone, bupr... Pharmacogenomics Established
rs3758581 CYP2C19 Ile331Val (CYP2C19*1B) Common CYP2C19 missense variant defining the *1B allele; the G (Val331) allel... Pharmacogenomics Moderate
rs3788189 SLC19A1 SLC19A1 IVS2 variant Intronic variant in the folate transporter gene associated with pemetrexed tr... Methylation & Detox Emerging
rs3791033 KDM4A Intronic variant in KDM4A histone demethylase associated with problematic opi... Pharmacogenomics Moderate
rs523349 SRD5A2 V89L Missense variant reducing 5-alpha-reductase type 2 enzyme activity, affecting... Hormones & Sleep Moderate
rs3814637 CYP2C19 Upstream CYP2C19 variant associated with altered R-warfarin clearance and inc... Pharmacogenomics Moderate
rs5030868 G6PD G6PD Mediterranean Severe Class II G6PD deficiency variant (c.563C>T, p.Ser188Phe) causing less ... Blood Sugar & Diabetes Established
rs3892097 CYP2D6 *4 CYP2D6 *4 splice-defect null allele — the most common loss-of-function CYP2D6... Pharmacogenomics Established
rs3918290 DPYD *2A Most critical pharmacogenomic variant causing complete loss of DPD enzyme fun... Pharmacogenomics Established
rs5219 KCNJ11 E23K Controls the pancreatic beta-cell potassium channel that regulates insulin se... Blood Sugar & Diabetes Strong
rs4148323 UGT1A1 *6 Gly71Arg Phase II glucuronidation enzyme that metabolizes bilirubin and many drugs inc... Pharmacogenomics Established
rs4149056 SLCO1B1 *5 Statin transport - affects muscle side effect risk with statins Pharmacogenomics Established
rs4244285 CYP2C19 *2 No-function CYP2C19 variant affecting PPIs, clopidogrel, and some antidepress... Pharmacogenomics Established
rs700518 CYP19A1 Val80 Synonymous variant in aromatase gene affecting estrogen production, bone dens... Hormones & Sleep Strong
rs4646438 CYP3A4 *6 (17776insA / frameshift) Frameshift insertion in CYP3A4 exon 9 that produces a truncated, non-function... Pharmacogenomics Strong
rs4646976 CYP2E1 CYP2E1 intronic haplotype tag — affects enzyme activity and susceptibility to... Pharmacogenomics Moderate
rs4986893 CYP2C19 *3 No-function CYP2C19 stop-gain variant — second most common loss-of-function a... Pharmacogenomics Established
rs4997557 CYP2A6 Rare CYP2A6 missense variant (p.Thr294Ile) that likely reduces nicotine-metab... Pharmacogenomics Emerging
rs5030655 CYP2D6 *6 Frameshift deletion causing no enzyme function, defining poor metabolizer sta... Pharmacogenomics Established
rs55785340 CYP3A4 *2 Missense variant reducing CYP3A4-mediated nifedipine clearance, causing eleva... Pharmacogenomics Moderate
rs55886062 DPYD *13 No-function DPYD star allele (I560S) causing severe DPD deficiency; one of fo... Pharmacogenomics Established
rs55897648 CYP2E1 *3 (Val389Ile) CYP2E1*3 missense variant with no demonstrated change in enzyme activity for ... Pharmacogenomics Emerging
rs56038477 DPYD HapB3 tag (c.1236G>A, E412E) Synonymous exon-11 tag SNP for the DPYD HapB3 haplotype; benign on its own bu... Pharmacogenomics Established
rs76723693 G6PD G6PD Nefza (c.968T>C) Missense variant in glucose-6-phosphate dehydrogenase causing Class III G6PD ... Blood Sugar & Diabetes Strong
rs58440431 CYP2D6 Intronic CYP2D6 variant tagging East Asian *10-lineage suballeles; the C alle... Pharmacogenomics Strong
rs622342 SLC22A1 A>C Intronic variant in the OCT1 organic cation transporter reducing hepatic metf... Pharmacogenomics Moderate
rs6413419 CYP2E1 *4 (V179I) Missense variant (Val179Ile) defining the CYP2E1*4 allele; associated with al... Pharmacogenomics Emerging
rs671 ALDH2 *2 Alcohol metabolism - flush reaction and cancer risk Pharmacogenomics Established
rs67376798 DPYD D949V Decreased-function variant reducing DPD enzyme activity ~30%, requiring 50% f... Pharmacogenomics Established
rs67784355 CYP3A4 *11 (Thr363Met) Rare missense variant in CYP3A4 that reduces protein expression and enzymatic... Pharmacogenomics Emerging
rs67807361 CYP2C9 p.Leu19Ile Rare CYP2C9 N-terminal missense variant of uncertain functional significance ... Pharmacogenomics Emerging
rs71328650 CYP2D6 Intronic CYP2D6 haplotype tag variant (rs28371702 canonical form) associated ... Pharmacogenomics Emerging
rs72547511 CYP1A2 CYP1A2*15 (Pro42Arg) Rare CYP1A2 missense variant at the critical Pro42 position; nearly abolishes... Pharmacogenomics Moderate
rs72547515 CYP1A2 *16 (Arg377Gln) Nearly-inactive CYP1A2 missense variant — carriers have severely impaired met... Pharmacogenomics Moderate
rs72547516 CYP1A2 Ile386Val Rare CYP1A2 missense variant (Ile386Val) associated with potentially reduced ... Pharmacogenomics Emerging
rs72547517 CYP1A2 *8 CYP1A2*8 — near-complete loss-of-function missense variant causing severely r... Pharmacogenomics Strong
rs72549354 CYP2D6 *20 Frameshift insertion creating a null CYP2D6 allele; carriers cannot metaboliz... Pharmacogenomics Established
rs75017182 DPYD HapB3 (c.1129-5923C>G) Deep intronic splice-site variant that is the functional driver of the DPYD H... Pharmacogenomics Established
rs762551 CYP1A2 *1F CYP1A2 *1F intronic inducibility variant — defines fast vs slow caffeine meta... Pharmacogenomics Strong
rs776746 CYP3A5 *3 Splice site variant creating a non-functional CYP3A5 enzyme, dramatically aff... Pharmacogenomics Established
rs8099917 IFNL3 Intergenic variant upstream of IFNL3 — second major IL28B locus predictor of ... Pharmacogenomics Established
rs8192780 CYP2E1 Downstream regulatory variant near CYP2E1 associated with nasopharyngeal carc... Pharmacogenomics Emerging
rs9923231 VKORC1 -1639G>A Warfarin sensitivity - determines initial dosing Pharmacogenomics Established